三苯基膦
光延反应
位阻效应
化学
产量(工程)
聚合物
反演(地质)
有机化学
材料科学
催化作用
生物
构造盆地
古生物学
冶金
作者
Jon White,Ashok Rao Tunoori,Debasree Dutta,Gunda I. Georg
出处
期刊:Combinatorial Chemistry & High Throughput Screening
[Bentham Science]
日期:2000-04-01
被引量:11
标识
DOI:10.2174/1386207003331706
摘要
Polymer-bound triphenylphosphine can replace triphenylphosphine in the Mitsunobu reaction to generate stereochemically inverted secondary alcohols. This method is comparable with the standard Mitsunobu reaction in terms of inversion of stereochemistry, yield, and reaction time, even for sterically very hindered secondary alcohols. The special merit of this reaction is that the excess polymer-bound triphenylphosphine and its by-products are easily removed by filtration from the reaction products.
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